Establishment of a novel chondrocyte-like cell line derived from transgenic mice harboring the temperature-sensitive simian virus 40 large T-antigen gene
- 1 November 1996
- journal article
- research article
- Published by Oxford University Press (OUP) in Journal of Bone and Mineral Research
- Vol. 11 (11) , 1646-1654
- https://doi.org/10.1002/jbmr.5650111108
Abstract
We established a clonal chondrocyte‐like cell line (TC6, TC stands for large T immortalized chondrocyte‐like cell line) derived from articular cartilage of transgenic mice harboring a temperature‐sensitive simian virus 40 large T‐antigen gene. TC6 cells exhibited spindle‐like or polygonal morphology and grew well at 33°C in alpha‐minimal essential medium supplemented with 0.5% fetal bovine serum. After confluence, these cells formed nodules that were positive for staining with alcian blue. Northern blot analysis demonstrated that these cells expressed messenger RNAs (mRNA) of the genes encoding cartilage‐specific proteins such as type II procollagen, link protein, and aggrecan. Furthermore, the expression of type II procollagen and link protein genes in TC6 cells was regulated by parathyroid hormone and basic fibroblast growth factor, suggesting the presence of the receptors for the hormone and cytokine. The expression of link protein mRNA in TC6 cells was regulated in a time‐dependent manner and was enhanced in culture within a week and increased continuously up to 10‐fold by the end of 4 weeks. Expression of mRNAs encoding type II procollagen and versican/PG‐M also increased moderately during the culture period. TC6 cells expressed type I procollagen mRNA, however, its level declined along with time in culture in contrast to the enhancement of the genes encoding cartilage‐specific molecules in these cells. Interestingly, alkaline phosphatase mRNA expression was barely detectable in the TC6 cells in their growing phase while it was enhanced dramatically more than 7‐fold by day 14 in culture. These results indicate that the TC6 cells could serve as an excellent model for the studies on chondrocyte physiology. (J Bone Miner Res 1996;11:1646–1654)Keywords
Funding Information
- Japanese Ministry of Education (068071 14 (N.M.), 05404053, 06044073, 07557096 (M.N.))
- Zimmer Research Foundation
This publication has 24 references indexed in Scilit:
- Development and characterization of a conditionally immortalized human fetal osteoblastic cell lineJournal of Bone and Mineral Research, 1995
- Type X collagen gene expression in mouse chondrocytes immortalized by a temperature-sensitive simian virus 40 large tumor antigen.The Journal of cell biology, 1995
- Interleukin-1 beta-modulated gene expression in immortalized human chondrocytes.Journal of Clinical Investigation, 1994
- In vivo effect of 1,25-dihydroxycholecalciferol on the proliferation and differentiation of avian chondrocytesJournal of Bone and Mineral Research, 1993
- Stable murine chondrogenic cell lines derived from c-fos-induced cartilage tumorsJournal of Bone and Mineral Research, 1993
- Regulation of expression of the chondrocytic phenotype in a skeletal cell line (CFK2) in vitroJournal of Bone and Mineral Research, 1993
- SV40‐immortalization of rabbit articular chondrocytes: Alteration of differentiated functionsJournal of Cellular Physiology, 1992
- Hepatocyte cell lines established from transgenic mice harboring temperature-sensitive simian virus 40 large T-antigen geneExperimental Cell Research, 1991
- An established rat cell line expressing chondrocyte propertiesExperimental Cell Research, 1988
- CartilagePublished by Elsevier ,1987